Recherche de Sous-structure

927

Clc1ccnc(Nc2ncco2)c1
Reaction #415
Rendement 0.5%
Clc1ccnc(Nc2ncco2)c1
Reaction #416
Rendement 7.7%
Cc1coc(Nc2cc(Cl)ccn2)n1
Reaction #422
Rendement 28.1%
Clc1ccnc(Nc2ncco2)c1
Reaction #453
Rendement 49.6%
Clc1ccnc(Nc2ncco2)c1
Reaction #454
Rendement 0.0%
Clc1ccnc(Nc2ncco2)c1
Reaction #455
Rendement 2.0%
Clc1ccnc(Nc2ncco2)c1
Reaction #456
Rendement 3.0%
Clc1ccnc(Nc2ncco2)c1
Reaction #457
Rendement 0.0%
Clc1ccnc(Nc2ncco2)c1
Reaction #458
Rendement 0.0%
Clc1ccnc(Nc2ncco2)c1
Reaction #459
Rendement 3.0%
Clc1ccnc(Nc2ncco2)c1
Reaction #460
Rendement 11.1%
Clc1ccnc(Nc2ncco2)c1
Reaction #461
Rendement 2.0%
Clc1ccnc(Nc2ncco2)c1
Reaction #462
Rendement 2.5%
c1ccc(Nc2ncco2)nc1
Reaction #672
Rendement 0.0%
c1ccc(Nc2ncco2)nc1
Reaction #673
Rendement 0.0%
c1ccc(Nc2ncco2)nc1
Reaction #674
Rendement 0.0%
CCOC(=O)c1coc(N(C)S(C)(=O)=O)n1
Reaction #42614
ethyl 2-[methyl(methylsulfonyl)amino]-1,3-oxazole-4-carboxylate
DOI: 10.6084/m9.figshare.5104873.v1
CN(c1nc(C(=O)O)co1)S(C)(=O)=O
Reaction #42615
2-[methyl(methylsulfonyl)amino]-1,3-oxazole-4-carboxylic acid
Rendement 82.4%DOI: 10.6084/m9.figshare.5104873.v1
CC(=O)N(C)c1nc2c(C#N)c(C)c(-c3ccccc3)c(N3CC[C@H](N(C)C)C3)c2o1
Reaction #45678
compound
Rendement 17.0%DOI: 10.6084/m9.figshare.5104873.v1
CCN(CC)c1nc2c(C#N)c(C)c(-c3ccccc3)c(N3CC[C@H](N(C)C)C3)c2o1
Reaction #45682
compound
Rendement 65.9%DOI: 10.6084/m9.figshare.5104873.v1
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